Related Experiment Video
Updated: Feb 17, 2026

11:25
3D Multicolor DNA FISH Tool to Study Nuclear Architecture in Human Primary Cells
Published on: January 25, 2020
11.0K
Feulgen staining remains the gold standard for precise DNA image cytometry
Stefan Biesterfeld1, Sascha Beckers, Maria Del Carmen Villa Cadenas
1Division of Cytopathology, Department of Pathology, Heinrich Heine University, Düsseldorf, Germany. Stefan.Biesterfeld@med.uni-duesseldorf.de
Anticancer Research
|January 29, 2011
Summary
Feulgen staining is the gold standard for DNA single-cell cytometry. Papanicolaou and hematoxylin stains produce unreliable DNA distribution histograms, hindering diagnostic conclusions.
Area of Science:
- Cytopathology
- Analytical Cytology
- Biomedical Imaging
Background:
- DNA single-cell cytometry is crucial for cancer diagnosis and prognosis.
- Accurate DNA content measurement relies on reliable staining techniques.
Purpose of the Study:
- To evaluate the suitability of Papanicolaou and hematoxylin staining for DNA single-cell cytometry.
- To compare these stains against the established Feulgen staining method.
Main Methods:
- Analyzed normal and cancerous cervical smears (n=20) using DNA single-cell cytometry.
- Measured integrated optical density (IOD) of 200 cells per sample.
- Compared DNA cytometric variables and nuclear area after Papanicolaou, hematoxylin, and Feulgen staining.
Main Results:
- Feulgen staining yielded regular DNA distribution histograms in normal cells.
- Papanicolaou and hematoxylin stains resulted in scattered DNA values and increased >4c populations.
- Dispersion parameters were significantly higher with Papanicolaou and hematoxylin compared to Feulgen staining.
Conclusions:
- Papanicolaou and hematoxylin staining are unsuitable for reliable DNA cytometry.
- Feulgen staining is confirmed as the gold standard for diagnostic and prognostic DNA content analysis.
Related Concept Videos
Karyotyping
68.7K
Overview
68.7K
Immunogold Electron Microscopy
5.6K
Immunoelectron microscopy utilizes immunogold labeling of endogenous proteins with specific antibodies to detect and localize these proteins in cells and tissues. The procedure provides insights into the distribution and quantification of protein under different stimulation conditions offering clues about their functions. Conjugating highly electron-dense gold particles with primary or secondary antibodies allow antigen detection on and within cells, with high resolution and specificity.
5.6K

